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        "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Algunos ni&#241;os contin&#250;an creciendo bien o experimentancrecimiento excesivo tras la extirpaci&#243;n de un craneo-faringioma&#44; a pesar de tener deficiencias de hormona delcrecimiento&#46; Presentamos el caso de una ni&#241;a diagnosticada a los 4 a&#241;os de craneofaringioma con extensi&#243;n supraselar&#46; Tras la intervenci&#243;n present&#243; hipopituitarismo m&#250;ltiple&#46; En los 5 a&#241;os siguientes creci&#243; entre 8&#44;4 y 10&#44;6 cm&#47;a&#241;o&#46; Despu&#233;s la velocidad de crecimiento disminuy&#243; progresivamente hasta 1&#44;2 cm&#47;a&#241;o&#44; increment&#225;ndose de nuevo a 9&#44;3 cm&#47;a&#241;o tras instaurar tratamiento con hormona del crecimiento&#46;</p>"
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                            0 => "J&#46;M&#46; Wit"
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                            2 => "S&#46; Van Buul-Offers"
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Vol. 53. Núm. 1.
Páginas 64-66 (julio 2000)
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Vol. 53. Núm. 1.
Páginas 64-66 (julio 2000)
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Hipercrecimiento y déficit de hormona del crecimiento tras tratamiento para el craneofaringioma
excessive growth and growth hormone deficiency after treatment for craniopharyngioma
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J.P. López Siguero*, E. García García, M.J. Martínez-Aedo y, A. Martínez Valverde
Departamento de Pediatría. Hospital Materno-Infantil Carlos Haya. Málaga
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Algunos niños continúan creciendo bien o experimentancrecimiento excesivo tras la extirpación de un craneo-faringioma, a pesar de tener deficiencias de hormona delcrecimiento. Presentamos el caso de una niña diagnosticada a los 4 años de craneofaringioma con extensión supraselar. Tras la intervención presentó hipopituitarismo múltiple. En los 5 años siguientes creció entre 8,4 y 10,6 cm/año. Después la velocidad de crecimiento disminuyó progresivamente hasta 1,2 cm/año, incrementándose de nuevo a 9,3 cm/año tras instaurar tratamiento con hormona del crecimiento.

Palabras clave:
Craneofaringioma
Crecimiento
Déficit de hormona del crecimiento

Some children grow normally or excessively after extirpation of a craniopharyngioma, despite growth hormone deficiency. We report a 4-year-old girl with suprasellar craniopharyngioma. Removal of the tumor resulted in panhypopituitarism. For the next 5 years growth continued at a rate of 8.4-10.6 cm/year and then decreased progressively to 1.2 cm/year. Administration of growth hormone increased growth rate to 9.3 cm/year.

Key words:
Craniopharyngioma
Growth
Growth hormone deficiency
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Bibliografía
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Copyright © 2000. Asociación Española de Pediatría
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